Few-Layered MoS2 Nanostructures for Highly Efficient Visible Light Photocatalysis

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650114 ◽  
Author(s):  
Dan Li ◽  
Jianwei Li ◽  
Caiqin Han ◽  
Xinsheng Zhao ◽  
Haipeng Chu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Electrochemical Impedance ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
Electrochemical Impedance Spectra ◽  
X Ray ◽  
Transmission Electron ◽  
Electron Hole Pair

Few-layered MoS2 nanostructures were successfully synthesized by a simple hydrothermal method without the addition of any catalysts or surfactants. Their morphology, structure and photocatalytic activity were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, electrochemical impedance spectra and UV-Vis absorption spectroscopy, respectively. These results show that the MoS2 nanostructures synthesized at 180[Formula: see text]C exhibit an optimal visible light photocatalytic activity (99%) in the degradation of Rhodamine B owing to the relatively easier adsorption of pollutants, higher visible light absorption and lower electron–hole pair recombination.

Hydrothermal Synthesis and Photocatalytic Properties of TiO2/SnS2 Nanocomposite

2014 ◽  
Vol 898 ◽  
pp. 23-26
Author(s):  
Jing Li ◽  
Wei Sun ◽  
Wei Min Dai ◽  
Yong Cai Zhang
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Diffuse Reflectance ◽  
Photocatalytic Property ◽  
Deionized Water ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Chloride Pentahydrate

TiO2/SnS2 nanocomposite was synthesized via hydrothermal treatment of tin (IV) chloride pentahydrate, thioacetamide and TiO2 nanotubes in deionized water at 150 °C for 3 h. The structure, composition and optical property of the as-synthesized nanocomposite were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy and UV-vis diffuse reflectance spectra, and its photocatalytic property was tested in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation. It was observed that TiO2 nanotubes exhibited no photocatalytic activity, whereas TiO2/SnS2 nanocomposite exhibited photocatalytic activity in the reduction of aqueous Cr6+ under visible-light (λ > 420 nm) irradiation.

scholarly journals Preparation of g-C3N4/MoS2 Composite Material and Its Visible Light Catalytic Performance

2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photogenerated Electron ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Calcination Method

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.

scholarly journals Direct Exfoliation of g-C3N4 with Addition of NaOH for Enhanced Photocatalytic Cr(Ⅵ) Reduction

2018 ◽  
Author(s):  
Yaping Guo ◽  
Jianyang Sun ◽  
Hui Chang ◽  
Xu Zhao
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
Physiochemical Properties ◽  
X Ray ◽  
Transmission Electron ◽  
Ultrasonic Process

A simple, effective and environmental-friendly method was adopted for enhancing the photocatalytic activity of g-C3N4 in the reduction of aqueous Cr(Ⅵ) under visible-light irradiation. The enhancement was achieved via treatment of g-C3N4 in organic solvent with addition of NaOH particles by ultrasonic process for two hours. The results demonstrated that the treated g-C3N4 exhibited much higher photocatalytic activity than pristine g-C3N4 in the reduction of Cr(VI) . Under visible light irradiation for 120 min, the reduced ratios of Cr(VI) with the initial concentration of 50 mg/L in the presence of the treated g-C3N4and pristine g-C3N4 were 100% and 37.1%, respectively. With the addition of fulvic acid, Cr(VI) was efficiently removed at 40 min. Based on the characterization results of the structures and other physiochemical properties of the treated g-C3N4 and pristine g-C3N4 by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV Vis diffuse reflectance, the possible reasons responsible for the enhanced photocatalytic activity of the treated g-C3N4 were proposed. The yield and mechanism of different exfoliation methods were compared by semi-quantitative method.

scholarly journals Controlled Synthesis of CuS and Cu9S5 and Their Application in the Photocatalytic Mineralization of Tetracycline

Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 899
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Damian C. Onwudiwe
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Blue Shift ◽  
X Ray Diffraction ◽  
X Ray ◽  
Copper Sulfides ◽  
Transmission Electron ◽  
Single Source Precursor ◽  
Pure Phase ◽  
Pure Phases

Pure-phase Cu2−xS (x = 1, 0.2) nanoparticles have been synthesized by the thermal decomposition of copper(II) dithiocarbamate as a single-source precursor in oleylamine as a capping agent. The compositions of the Cu2−xS nanocrystals varied from CuS (covellite) through the mixture of phases (CuS and Cu7.2S4) to Cu9S5 (digenite) by simply varying the temperature of synthesis. The crystallinity and morphology of the copper sulfides were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), which showed pure phases at low (120 °C) and high (220 °C) temperatures and a mixture of phases at intermediate temperatures (150 and 180 °C). Covellite was of a spherical morphology, while digenite was rod shaped. The optical properties of these nanocrystals were characterized by UV−vis–NIR and photoluminescence spectroscopies. Both samples had very similar absorption spectra but distinguishable fluorescence properties and exhibited a blue shift in their band gap energies compared to bulk Cu2−xS. The pure phases were used as catalysts for the photocatalytic degradation of tetracycline (TC) under visible-light irradiation. The results demonstrated that the photocatalytic activity of the digenite phase exhibited higher catalytic degradation of 98.5% compared to the covellite phase, which showed 88% degradation within the 120 min reaction time using 80 mg of the catalysts. The higher degradation efficiency achieved with the digenite phase was attributed to its higher absorption of the visible light compared to covellite.

Enhanced visible-active photocatalytic behaviors observed in Mn-doped BiFeO3

2018 ◽  
Vol 32 (17) ◽  
pp. 1850185 ◽  
Author(s):  
Yun-Hui Si ◽  
Yu Xia ◽  
Ya-Yun Li ◽  
Shao-Ke Shang ◽  
Xin-Bo Xiong ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Band Gap ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Mn Doped ◽  
Hole Recombination ◽  
Narrow Band Gap Semiconductors

A series of BiFeO3 and BiFe[Formula: see text]Mn[Formula: see text]O3 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.10) were synthesized by a hydrothermal method. The samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy (EDS) and UV–Vis diffuse reflectance spectroscopy, and their photocatalytic activity was studied by photocatalytic degradation of methylene blue in aqueous solution under visible light irradiation. The band gap of BiFeO3 was significantly decreased from 2.26 eV to 1.90 eV with the doping of Mn. Furthermore, the 6% Mn-doped BiFeO3 photocatalyst exhibited the best activity with a degradation rate of 94% after irradiation for 100 min. The enhanced photocatalytic activity with Mn doping could be attributed to the enhanced optical absorption, increment of surface reactive sites and reduction of electron–hole recombination. Our results may be conducive to design more efficient photocatalysts responsive to visible light among narrow band gap semiconductors.

Ag2O/ZnO Heterostructures with Enhanced Photocatalytic Activity

2021 ◽  
Vol 1035 ◽  
pp. 1043-1049
Author(s):  
Di Xiang ◽  
Chang Long Shao
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Environmental Remediation ◽  
Organic Dyes ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
P Type

A simple route has been developed for the synthesis of Ag2O/ZnO heterostructures and the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS) and photoluminescence (PL) spectroscopy analysis. Considering the porous structure of Ag2O/ZnO, the photocatalytic degradation for the organic dyes, such as eosin red (ER), methyl orange (MO), methylene blue (MB) and rhodamine B (RhB), under visible light irradiation was investigated in detail. Noticeably, Ag2O/ZnO just took 40 min to degrade 96 % MB. The rate of degradation using the Ag2O/ZnO heterostructures was 2.3 times faster than that of the bare porous ZnO nanospheres under visible light irradiation due to that the recombination of the photogenerated charge was inhibited greatly in the p-type Ag2O and n-type ZnO semiconductor. So the Ag2O/ZnO heterostuctures showed the potential application on environmental remediation.

Laccase Biosensor Based on Ag-Doped TiO2 Nanoparticles on CuCNFs for the Determination of Hydroquinone

NANO ◽  
2016 ◽  
Vol 11 (12) ◽  
pp. 1650132 ◽  
Author(s):  
Jie Yang ◽  
Dawei Li ◽  
Zengyuan Pang ◽  
Qufu Wei
Keyword(s):  
Electron Microscopy ◽  
Storage Stability ◽  
Electrochemical Impedance ◽  
The Novel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
New Material ◽  
And Storage

A novel nanomaterial composed of copper and carbon nanofibers (CuCNFs) decorated with Ag-doped TiO2 (Ag–TiO[Formula: see text] nanoparticles was prepared through electrospinning, carbonization and solvothermal treatment. The composites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and electrochemical impedance spectroscopy (EIS). The obtained composites were mixed with laccase and Nafion to construct novel hydroquinone biosensor. The electrochemical behavior of the novel biosensor was studied using cyclic voltammetry (CV) and chronoamperometry. The results demonstrated that the biosensor possessed a wide detection linear range (1.20–176.50[Formula: see text][Formula: see text]M), a good selectivity, repeatability, reproducibility and storage stability. This work provides a new material to design more efficient laccase (Lac) based biosensor for hydroquinone detection.

scholarly journals Incorporation of reduced graphene oxide into faceted flower-like {001} TiO 2 for enhanced photocatalytic activity

2018 ◽  
Vol 5 (8) ◽  
pp. 180613 ◽  
Author(s):  
Haijin Liu ◽  
Peiyao Li ◽  
Haokun Bai ◽  
Cuiwei Du ◽  
Dandan Wei ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Graphene Oxide ◽  
Visible Light ◽  
Reduced Graphene Oxide ◽  
Theoretical Calculations ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Photocatalytic Activities

Anatase TiO 2 with {001} facets is much more active than that with {101} facets, which has been verified via experiments and theoretical calculations. Graphene has garnered much attention since it was initially synthesized, due to its unique properties. In this study, reduced graphene oxide (RGO)/{001} faceted TiO 2 composites were fabricated via a solvothermal method. The composites were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectrophotometry, photoluminescence and Raman analysis. The results revealed that the graphene oxide was reduced during the preparation process of the {001} faceted TiO 2 , and combined with the surface of {001} TiO 2 . The photocatalytic activities of the composites were evaluated through the degradation of basic violet, under both white light ( λ > 390 nm) and visible light ( λ = 420 nm) irradiation. The results indicated that the photocatalytic activities of the {001} faceted TiO 2 were significantly improved following the incorporation of RGO, particularly under visible light irradiation. Theoretical calculations showed that the band structure of the {001} faceted TiO 2 was modified via graphene hybridization, where the separation of photoinduced electron–hole pairs was promoted; thus, the photocatalytic activity was enhanced.

Hydrothermal Synthesis of Visible Light Active SnO2-SnS2 Nanocomposite Photocatalyst for the Reduction of Cr(VI) in Water

2013 ◽  
Vol 709 ◽  
pp. 7-10
Author(s):  
Jing Li ◽  
Xi Hua Du ◽  
Wei Min Dai ◽  
Yong Cai Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Sno2 Nanoparticles ◽  
High Photocatalytic Activity ◽  
X Ray ◽  
Transmission Electron ◽  
Visible Light Active ◽  
Composition Structure

A low temperature (130 °C) hydrothermal method was proposed for the synthesis of SnO2-SnS2 nanocomposite. The composition, structure and optical property of the as-synthesized SnO2-SnS2 nanocomposite were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy, high-resolution transmission electron microscopy and UV-vis diffuse reflectance spectra, and its photocatalytic activity was tested by the reduction of Cr(VI) in water under visible light (λ > 420 nm) irradiation. It was found that the as-synthesized SnO2-SnS2 nanocomposite exhibited high photocatalytic activity in the reduction of Cr(VI) in water under visible light (λ > 420 nm) irradiation, whereas SnO2 nanoparticles displayed no photocatalytic activity in the reduction of Cr(VI) in water under visible light (λ > 420 nm) irradiation.

Hydrothermal Synthesis and Photocatalytic Properties of Flower-Like CdS Nanostructures

2011 ◽  
Vol 335-336 ◽  
pp. 460-463 ◽  
Author(s):  
Hong Mei Wang ◽  
Da Peng Zhou ◽  
Yuan Lian ◽  
Ming Pang ◽  
Dan Liu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Sulfur Source ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Transmission Electron ◽  
Cds Nanostructures

Hexagonal flower-like CdS nanostructures were successfully synthesized through a facile hydrothermal method with thiourea as sulfur source. By combining the results of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), the structural and morphological characterizations of the products were performed. The photocatalytic activity of CdS nanostructures had been tested by degradation of Rhodamine B (RB) under UV light compared to commercial CdS powders, which indicated that the as-syntherized CdS nanostructures exhibited enhanced photocatalytic activity for degradation of RB. The possible growth mechanism of CdS nanostructures was proposed in the end.

Sign in / Sign up

Export Citation Format

Share Document